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Neurofibromatosis:     more books (99)

Plexiform neurofibromatosis (Recklinghausen's disease) or orbit and globe with associated glioma of the optic nerve and brain report of a case by Frederick Allison Davis, 1939 Neurofibromatosis Phenotype, Natural History, and Pathogenesis Multiple neurofibromatosis (von Recklinghausen's disease) and its inheritance: With descriptions of a case, (Eugenics record office.Bulletin) by Samuel Aaron Preiser, 1918 The child with neurofibromatosis 1 by Bruce R Korf, 1991 Neurofibromatosis: Information for kids by Elizabeth Collins, 1986 Neurofibromatosis (A Handbook for Patients, Families, and Health Care Professionals) by Allen E. Rubenstein Bruse R. Korf, 2005 Neurofibromatosis 2 (bilateral acoustic neurofibromatosis) by Robert L Martuza, 1988 Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (Bilateral acoustic neurofibromatosis) : an upate (SuDoc HE 20.3002:N 39/4) by U.S. Dept of Health and Human Services, Neurofibromatosis Multiple Neurofibromatosis, a Clinical, Pathological, and Genetic Study of; by Frank, Et Al; Crowe, 1956 ON NEUROMA AND NEuRO-FIBROMATOSIS by Alexis THOMSON, 1900 Clinical and Genetic Investigations into Tuberous Sclerosis and Recklinghausen's Neurofibromatosis: Contribution to Elucidation of Interrelationship and Eugenics of the Syndromes. Acta Psychiatriaca et Neurologica Scandinavica Supplementum 71 by Allan Borberg, 1951 Neurofibromatosis in childhood (Current problems in pediatrics) by David W Dunn, 1987 Neurofibromatosis by Vincent M. (MD) and Eichner, June E. Riccardi, 1986-01-01

lists with details

81. THE MERCK MANUAL--SECOND HOME EDITION, Neurofibromatosis In Ch. 88, Tumors Of Th
    About half of the people with neurofibromatosis inherit it. No known treatment can stop the progression of neurofibromatosis or cure it.  
    http://www.merck.com/mmhe/sec06/ch088/ch088d.html
    
    Extractions: var externalLinkWarning = "The link you have selected will take you to a site outside Merck and The Merck Manuals.*n*nThe Merck Manuals do not review or control the content of any non-Merck site. The Merck Manuals do not endorse and are not responsible for the accuracy, content, practices, or standards of any non-Merck sources."; Search The Second Home Edition , Online Version Search Index A B C D ... Z Sections Accidents and Injuries Blood Disorders Bone, Joint, and Muscle Disorders Brain, Spinal Cord, and Nerve Disorders ... Women's Health Issues Resources Anatomical Drawings Multimedia Pronunciations Weights and Measures ... , Online Version Section Brain, Spinal Cord, and Nerve Disorders Chapter Tumors of the Nervous System Topics Introduction Brain Tumors Neurofibromatosis Radiation Damage Spinal Cord Tumors Neurofibromatosis Buy The Book Print This Topic Email This Topic Pronunciations acoustic neuroma fibroma meningioma neurofibromatosis ... neuroma Neurofibromatosis is a genetic disorder in which many soft, fleshy growths of nerve tissue (neurofibromas) grow under the skin and in other parts of the body. Symptoms and Diagnosis About one third of people with peripheral neurofibromatosis notice no symptoms, and the disorder is first diagnosed during a routine examination when doctors find lumps under the skin near nerves. Another third of the people seek help for a cosmetic problem caused by the disorder, leading to its diagnosis. In the remaining third, the disorder is diagnosed when people notice neurologic problems, such as weakness due to compression of the spinal cord or nerves.

82. Neurofibromatosis
    Online health news and information for consumers.  
    http://www.health-news-and-information.com/4cfvhs/libv/i63.shtml
    
    Extractions: 1638 Owen Dr. Fayetteville, NC 28304 (910) 609-4000 Heart Cancer Women Men ... All Health Topics A-Z Neurofibromatosis is a complicated genetic disease that can affect both men and women in all races and ethnic groups. The neurofibromatoses are a set of genetic disorders that cause tumors to grow on and along various types of nerves. The tumors can grow anywhere on or in the body. The disease can also affect non-nervous tissues like bones and skin and lead to developmental abnormalities such as learning disorders, according to the National Neurofibromatosis Foundation (NNFF). Scientists have classified Neurofibromatosis (NF) into two distinct types: Both forms are genetic disorders that may be inherited from a parent, but according to the National Institute of Neurological Disorders and Stroke (NINDS), 30 to 50 percent of the cases are the result of a gene mutation in an individual rather than being inherited. Neurofibromatosis Type 1 (NF1) This is the more common type of the neurofibromatoses, occurring in 1 in 4,000 births. It is sometimes called Von Recklinghausen NF or Peripheral NF. In most cases, symptoms of NF1 are mild, and patients live normal and productive lives. In some cases, however, NF1 can be severely debilitating. It is mainly characterized by multiple light brown spots (called café-au-lait spots) and neurofibromas (nerve tumors) on or under the skin. It can also cause bone defects and curvature of the spine (scoliosis). (Read about "

83. Your Child | Neurofibromatosis
    There are two distinct forms of neurofibromatosis NF1 and NF2. What is neurofibromatosis1? neurofibromatosis 1 (NF1) is the most common type of  
    http://www.med.umich.edu/1libr/yourchild/neurofib.htm
    
    Extractions: What is Neurofibromatosis? Neurofibromatosis (NF) , also known as von Recklinghausen disease , is a common autosomal dominant disorder that can affect many organs in the body, especially the skin and the nervous system .  Some of the features may be present at birth, but others do not appear for many years.  There are two distinct forms of Neurofibromatosis:  and What is Neurofibromatosis-1? Neurofibromatosis 1 (NF1) is the most common type of Neurofibromatosis, and it is seen in 1/4000 people.  It is characterized by multiple birthmarks as well as tumors in the nervous system and brain.  It is often inherited in an autosomal dominant fashion, however, in 50% of cases there is no family history and it is a result of a gene mutation , a new change not seen in other family members. What is Neurofibromatosis-2?

84. AllRefer Health - Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis (BAN
    neurofibromatosis 2 (Bilateral Acoustic neurofibromatosis (BAN), Central Bilateral Acoustic NF, NF2) information center covers causes, prevention, symptoms,  
    http://health.allrefer.com/health/neurofibromatosis-2-info.html
    
    Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia

85. Healthfinder® - Neurofibromatosis
    Carefully selected government and nonprofit health information on neurofibromatosis.  
    http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=577

86. University Of Chicago Comer Children's Hospital: Neurofibromatosis
    This information is for families who have recently been told that one member may have neurofibromatosis (NF).  
    http://www.uchicagokidshospital.org/specialties/neurology/patient-guides/neurofi

87. Neurofibromatosis
    neurofibromatosis Type 1 and Type 2 A Comprehensive Overview neurofibromatosis (NF) is a genetic disorder that is inherited in an autosomal dominant  
    http://www.smsu.edu/nursing/geneticsinnursing/neurofibromatosis.htm
    
    Extractions: The incidence for NF type 2 (NF2) is rare, and estimated at 1:35,000-40,000 births (Evans, 1999). The incidence rate for NF2 is estimated because the disease is rare and can often go undiagnosed. Because the incidence of the other six types is more rare than NF2, only NF1 and NF2 will be discussed in this paper. Neurofibromatosis Type 1 is a distinct disease that is diagnosed by symptoms. The classic symptoms being more than 6 café-au-lait spots, inguinal/axillary freckling, and neurofibromas (Gutmann, et al., 1997). There are several clinical manifestations for people with NF1. Many have optic gliomas, learning disabilities, plexiform neuromas, growth or hormone disorders, hypertension, and glaucoma. The symptoms of the disease may vary from mild to severe. The progression of the disease will vary from slow to rapid. Some people will have no progression, where as others will have extensive involvement early in the clinical picture. Treatment is based on symptoms. It is recommended that people with NF1 be referred to a geneticist and other physicians who has experience with the disease for an initial evaluation. The primary care provider can then direct follow up.

88. Neurofibromatosis (NF) Clinical Program : St. Louis Children's Hospital
    The neurofibromatosis Comprehensive Care Team provides detailed patient assessments and works with referring physicians, allied health professionals and  
    http://www.stlouischildrens.org/default.aspx?tabid=89&acn=view&aid=3477

89. NF1
    However, persons with neurofibromatosis have a longterm risk for development of malignant neoplasms neurofibrosarcomas, malignant schwannomas, gliomas.  
    http://medgen.genetics.utah.edu/photographs/pages/nf1.htm
    
    Extractions: view 6 KB version A young adult with multiple dermal neurofibromas of the trunk. Note also a cafe-au-lait spot in the right upper abdomen. This picture shows a body with several neurofibromas. Seen here are multiple nodules on the skin surface of the forearm and hand of a patient with neurofibromatosis. The yellow-orange staining of the skin is betadine solution applied in surgery, as this is an amputation specimen. A neurofibrosarcoma was present in the deep soft tissue of the wrist. Microscopically, the skin overlying a neurofibroma may show some hyperpigmentation, but the actual lesion is in the dermis. The neurofibroma consists of bundles of wavy spindle cells with a lot of intervening pink collagen. At higher magnification, the neurofibroma is seen to have elongated wavy cells with small dark oblong nuclei. This lesion is benign. However, persons with neurofibromatosis have a long-term risk for development of malignant neoplasms: neurofibrosarcomas, malignant schwannomas, gliomas. Close-up of a cutaneous neurofibroma surrounding by freckles in an individual with neurofibromatosis type 1.

90. PN Tumors
    neurofibromatosis 1; neurofibromatosis 2 Especially vestibular Schwannomas Neural crest tumors without neurofibromatosis May have acquired somatic  
    http://www.neuro.wustl.edu/neuromuscular/nanatomy/pntumor.htm
    
    Extractions: Tumor-like disorders Morton's (Plantar neuroma) Pathology: Fibrosis of plantar digital nerve Amputation neuroma Nerve sheath ganglion (Cyst) Neuromuscular hammartoma (Benign Triton tumor) Mucosal neuroma Palisaded encapsulated neuroma Onset: Middle age Benign Neurothekoma Onset: Young females Benign Pathology subtypes Ganglion cyst Benign Treatment Lipoma Benign MRI: May be diagnostic Treatment: Dependent on whether the lipoma is intrinsic or extrinsic to nerve Intrinsic: Biopsy or Release entrapment; Avoid nerve damage

91. Multiple Neurofibromatosis
    Multiple neurofibromatosis (Von Recklinghausen´s Disease) multiple neurofibromatosis. neurofibroma. Etiology. genetic. Tissue of Origin. nerve tissue  
    http://www.dental.mu.edu/oralpath/lesions/neurofibromatosis/neurofibromatosis.ht
    
    Extractions: Clinical Features: adults no sex predilection slow-growing, soft, painless lesions size varies multiple neurofibromas in the oral cavity and on the skin of the skin Radiographic Features: well-demarcated unilocular or multilocular radiolucency. possible root disturbance possible jaw enlargement Differential Diagnosis: multiple neurofibromatosis neurofibroma Etiology: genetic Tissue of Origin: nerve tissue Histologic Features: haphazardly scattered spindle shaped Schwann cells mast cells are present variants: myxoid neurofibromas plexiform neurofibromas nerve sheath myxomas Main Pathologic Process: benign neoplasia Treatment: surgical excision but may be impractical due to the number of lesions best left untreated because multiple recurrences may be associated with malignant transformation to neurogenic sarcoma Prognosis: may recur

92. ► Neurofibromatosis-2
    A medical encycopedia article on the topic neurofibromatosis-2.  
    http://www.umm.edu/ency/article/000795.htm

93. Principles Of Pediatric Dermatology - Chapter 32 : GENODERMATOSES
    Elephantiasis neurofibromatosa is a similar diffuse neurofibromatosis of nerve trunks Other malignant diseases associated with neurofibromatosis include  
    http://www.drmhijazy.com/english/chapters/chapter32.htm
    
    Extractions: This chapter summarizes some of the genetic syndromes associated with cutaneous manifestations. Some of these syndromes are rare and usually appear early in life .These syndromes are included in this text on belief that one time or one-day some of these syndromes may be faced during medical practice. It would be hard for the physician at that time to be confused in front of his patient having nothing to do or to tell. General considerations Genodermatoses is referred to a group of diseases which are due to genetically determined disorders. A congenital abnormality which is present at or before birth, is not necessarily genetically determined. A congenital defect : may be as a result of an infection from the mother or an abnormality in the development, which is not genetically related. Not all inherited disorders are congenital ; they may not become apparent until late childhood or even old age.

94. Neurofibromatosis Support Group Of Solano County
    January 2004. Our two year old son, Carter, was diagnosed with a spontaneous mutation of neurofibromatosis (NF) when he was two months old.  
    http://www.nfnocal.org/

95. BrainTalk Communities - Neurofibromatosis
    Reload this Page neurofibromatosis. User Name, Remember Me? Password Threads in Forum neurofibromatosis, Forum Tools, Search this Forum. Announcement  
    http://brain.hastypastry.net/forums/forumdisplay.php?f=190

96. Café-au-lait Spots And Neurofibromatosis - DrGreene.com
    When should a parent worry that cafeau-lait spots are a sign of neurofibromatosis? Pediatrician Alan Greene, MD, discusses the symptoms of  
    http://www.drgreene.com/21_80.html
    
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97. MyDNA.com - Neurofibromatosis
    myDNA is a consumer focused health, genetics, and genomics information provider offering disease condition information, health wellness tips,  
    http://www.mydna.com/genes/genetics/disorders/disease/cancer/neurofibromatosis.h
    
    Extractions: Page Tools Print This Page E-Mail This Page Add to Favorites Genetics Genetics News Ask Dr. DNA Top Tens Genetics 101 Genetic Testing Genetic Disorders Genes and Disease Blood Diseases Cancer Digestive System Ear, Nose and Throat Female-Specific Disease Glands and Hormones Heart and Blood Vessels Immune System Male Specific Disease Muscle and Bone Neonatal Diseases Nervous System Nutritional and Metabolic Respiratory Diseases Skin, Connective Tissue

98. Neurofibromatosis
    neurofibromatosis is an autosomal dominant inherited disorder that affects about one in 3000 individuals. The expression of the gene is variable,  
    http://www.drhull.com/EncyMaster/N/neurofibromatosis.html
    
    Extractions: Help for sleepless parents Encyclopedia Index N neurofibromatosis Search neurofibromatosis Neurofibromatosis is an autosomal dominant inherited disorder that affects about one in 3,000 individuals. The expression of the gene is variable, meaning that carriers of the disease may be more or less severely affected. Also, there is a high rate of mutation , which means that many new cases arise spontaneously in the embryo and are not inherited from the parents. The hallmark of the disease is the formation of neurofibromas, tumors which arise from any of the nerve types of the body. These tumors can occur anywhere in the body, including within any of the bones. It may be associated with varying degrees of mental retardation, which is related to the underlying disease and not the tumors. The tumors are almost all benign, but may degenerate into malignancies later in life. This disease has an extraordinary variability in its manifestation. A variety of different types of tumors can arise in the skin, nervous system, or in the bones, with a multitude of possible complications. The ususal course of the disease is the appearance in infancy of multiple cafe-au-lait spots. Characteristic skin manifestations appear during childhood or around puberty. These are cafe-au-lait spots or pigmented nevi (common moles). Eventually the adult individual may exhibit the characteristic multiple pendulous masses of skin and fibrous tissue most people associate with the disease.

99. DermIS / Main Menu / DOIA / Alphabetically / Diagnosenames Containing 'neurofibr
    alphabetically / diagnosenames containing neurofibromatosis neurofibromatosis, 21. neurofibromatosis Generalisata (von Recklinghausen), 21  
    http://www.dermis.net/doia/abrowser.asp?zugr=d&lang=e&beginswith=neurofibromatos

100. NEUROFIBROMATOSIS
     Aneurofibromatosis type 1. B-neurofibromatosis type 2. C-neurofibromatosis type 3. D-Tuberous sclerosis. E-von Hippel-Lindau Disease  
     http://www.mcl.tulane.edu/classware/pathology/medical_pathology/neuropathology/n

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